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of Volume 4 -- 1 Alcohol Use in Tribal Societies -- 2 Anthropological Perspectives on the Social Biology of Alcohol: An Introduction to the Literature -- 3 Drinking Behavior and Drinking Problems in the United States -- 4 Alcoholism in Women -- 5 Youthful Alcohol Use, Abuse, and Alcoholism -- 6 Family Structure and Behavior in Alcoholism: A Review of the Literature -- 7 The Alcoholic Personality -- 8 Alcoholism and Mortality -- 9 Alcohol and Unintentional Injury -- 10 Alcohol and Crimes of Violence -- 11 Alcohol Abuse and Work Organizations -- 12 Education and the Prevention of Alcoholism -- 13 The Effects of Legal Restraint on Drinking.

Background: Voltage of the P300 component of eventrelated potentials (ERPs) has been proposed as a phenotypic marker of risk for alcoholism. P3a elicited by intrusive events is important in the context of deficits in inhibition found during psychophysiological and behavioral evaluations in children of alcoholics. Methods: ERPs were recorded from a group of adult children of alcoholics (n 5 26) and controls (n 5 23) with a three-stimulus visual oddball paradigm. The task required a difficult perceptual discrimination between a frequent (.80) vertical line and an infrequent (.10) 2° tilted line (target). An easily discriminable nontarget infrequent horizontal line also occurred (.10). Subjects were required to press a button to the target. P3a was compared using mixed-model ANCOVAs at 31 sites organized in 5 scalp regions. Current source density (CSD) maps were also analyzed. Results: High-risk (HR) subjects manifested reduced P3a amplitudes compared to controls at frontal, central, parietal, and temporal electrodes. CSD analyses supported these findings with group differences found for all the scalp regions. Conclusions: The results are discussed in relation to previous HR studies. P3a reductions may be related to deficits in neuronal inhibition during stimulus processing. These results suggest that P3a amplitude may be important as a marker for vulnerability to alcoholism. ; This research was supported by NIH Grants AA08401 and AA08403. Dr. Holguin is a Visiting Research Fellow at the Department of Psychiatry, State University of New York Health Science Center, supported by the Galician Government Research Authority (DOG 08/26/1997) ; SI